[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"telehealth\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:telehealth":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,43,70,108,140,169,200,225],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100644990","oncologic-timely-palliative-care-and-remote-monitoring-with-electronic-assessments-and-telehealth-on-target-100644990",false,"NCT07674797","Oncologic Timely Palliative Care And Remote Monitoring With Electronic Assessments And Telehealth (ON-TARGET)","Eligibility Criteria\n\n* Age ≥ 18\n* Outpatients who are within 12 weeks of diagnosis of metastatic solid tumors and seen by one of the participating medical oncologists\n* Eastern Cooperative Oncology Group Performance Status 0.2\n* Able to speak English or Spanish\n\nExclusion Criteria:\n\n. Cognitive impairment in the opinion of the oncologist necessitating need for a surrogate decision making.\n\n• Previously seen by SPC team at UT MD Anderson","ALL","18 Years",{"count":18,"type":19},300,"ESTIMATED","INTERVENTIONAL",[22],"NA","To examine how we can provide supportive care for patients with advanced cancer better tailored to their needs",[25,26,27,28,29],"Oncologic","Palliative Care","Remote Monitoring","Electronic Assessments","Telehealth","NOT_YET_RECRUITING","2026-06-24",{"date":33,"type":34},"2026-06-30","ACTUAL",{"date":36,"type":19},"2026-11-22",{"date":38,"type":19},"2034-06-30",{"name":40,"class":41},"M.D. Anderson Cancer Center","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":15,"minAge":51,"maxAge":4,"enrollmentInfo":52,"targetDuration":4,"studyType":20,"phases":54,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":60,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":42},"100595579","modifying-the-geriatric-acute--post-acute-care-coordination-program-for-fall-prevention-in-the-emergency-department-for-telehealth-100595579","NCT07034287","Modifying the Geriatric Acute & Post-acute Care Coordination Program for Fall Prevention in the Emergency Department for Telehealth","eGAPcare: Modifying the Geriatric Acute & Post-acute Care Coordination Program for Fall Prevention in the Emergency Department for Telehealth","eGAPcare","Inclusion Criteria:\n\n* Community-dwelling adult (non-institutionalized) 65 years-old or older presenting to ED after a fall\n* Fall not due to syncope or external force (i.e., struck by car or assault)\n* Fall not due to serious illness (i.e., stroke, acute myocardial infarction)\n* Will be discharged to home\u002Fassisted living\u002Frehabilitation at completion of ED visit (i.e., not admitted)\n* Proxy available to give informed consent if patient lacks capacity\n\nExclusion Criteria:\n\n* Unable to give informed consent due to intoxication or acute change in mental status\n* Presence of injuries that prevent mobilization (i.e., pelvic or lower extremity fractures)","65 Years",{"count":53,"type":19},40,[22],"The goal of this clinical trial is to determine the feasibility of eGAPcare, a telehealth modification of the GAPcare fall prevention intervention, in older adults in a community emergency department. The main questions it aims to answer are:\n\n* Can telehealth physical therapy and pharmacy consultations be conducted in a community emergency department?\n* Does the telehealth modification of GAPcare decrease recurrent falls at 6 months? Participants will\n* Receive telehealth physical therapy and pharmacy consultation while in the emergency department\n* Participate in follow-up visits over the phone for 6 months following the initial emergency department visit\n* Complete study questionnaires delivered by study staff.",[57,58,29,59],"Older Adults (65 Years and Older)","Fall Prevention","Emergency Department","RECRUITING","2026-02-09",{"date":63,"type":34},"2026-02-11",{"date":65,"type":34},"2026-01-13",{"date":67,"type":19},"2027-01-01",{"name":69,"class":41},"University of Colorado, Denver",{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":76,"eligibilityCriteria":77,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":78,"enrollmentInfo":79,"targetDuration":4,"studyType":20,"phases":81,"briefSummary":82,"conditions":83,"keywords":95,"overallStatus":60,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":106,"locationsCount":42},"100531998","the-fit-with-us-study-100531998","NCT06207084","The Fit With Us Study","Precision-based Teleexercise Trial to Increase Adherence in People With Disabilities","FITWITHUS","Eligible participants must meet the following criteria to be included: (1) live with a permanent physical disability that limits their mobility; (2) be 18 to 89 years of age; (3) have broadband internet access; (4) be able to speak and read English; and (5) be able to attend coaching and training sessions during the weekdays.\n\nParticipants are excluded from participation if they (1) possess significant visual acuity that prevents seeing a computer screen to follow a home exercise program; (2) have been regularly engaging in exercise for the previous 3 months; (3) are unable to use their arms and their legs at all to exercise; (4) are unsafe to exercise; (5) self-report that they are currently pregnant","89 Years",{"count":80,"type":19},257,[22],"The purpose of this 32-week study is to use an innovative experimental design known as SMART (Sequential Multiple Assignment Randomized Trial), which will allow us to determine the best way to sequence the delivery of teleexercise (referred to as an adaptive intervention), combined with predictive analytics on participant adherence in a stepped program of physical activity interventions. All 257 participants will have access to a library of recorded video exercise content, and a weekly wellness article. Some participants will receive health coaching calls (1st randomization). Analytic data will be used to determine which participants are responding or not responding to the intervention. Participants not responding after 4 weeks will receive either live one-on-one or group exercise training (2nd randomization). After 8 weeks, the participant will receive only pre-recorded exercise content and articles for a 24-week maintenance phase (weeks 9-32). The study outcomes are: The effectiveness of the adaptive interventions; Exploring mediating and moderating variables; Sensitivity analysis of the predictive analytics.",[84,85,29,86,87,88,89,90,91,92,93,94],"Mobility Limitations","Disability Physical","Health Coaching","Physical Activity","Behavior, Health","eHealth","Health Literacy","Self Efficacy","Fatigue","Usability","Predictive Model",[96,97,98],"telehealth","health coaching","disability","2026-01-07",{"date":101,"type":34},"2026-01-09",{"date":103,"type":34},"2024-09-01",{"date":105,"type":19},"2029-02-01",{"name":107,"class":41},"University of Alabama at Birmingham",{"id":109,"slug":110,"hasResults":11,"nctId":111,"briefTitle":112,"officialTitle":112,"acronym":113,"eligibilityCriteria":114,"healthyVolunteers":11,"sex":115,"minAge":16,"maxAge":116,"enrollmentInfo":117,"targetDuration":4,"studyType":20,"phases":119,"briefSummary":120,"conditions":121,"keywords":125,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":131,"lastUpdatePostDateStruct":132,"startDateStruct":134,"completionDateStruct":136,"leadSponsor":138,"locationsCount":42},"100615525","the-impact-of-virtual-doula-services-on-birth-outcomes-in-rural-communities-100615525","NCT07293741","The Impact of Virtual Doula Services on Birth Outcomes in Rural Communities","RIVER","Inclusion Criteria:\n\n* 18-45 years of age\n* pregnant (second or early third trimester) with their first child\n* reside in a rural zip codes in the U.S.\n\nExclusion Criteria:\n\n* non-singleton pregnancy\n* police custody or incarceration\n* infant to be separated from mother (e.g., placed for adoption, protective custody)\n* working with a doula prior to enrollment.","FEMALE","45 Years",{"count":118,"type":19},614,[22],"This study will assess the impact of virtual doula care on birth and postnatal outcomes among rural mothers. The goal of virtual doula services is to improve access to care in underserved communities and decrease urban-rural differences in key maternal health outcomes including mode of birth (cesarean vs vaginal) and birth satisfaction. By implementing a digital randomized controlled trial, the study team will efficiently recruit a national sample of rural pregnant women to provide evidence of the effectiveness of virtual doula care, the appropriateness of virtual visits for different care and support needs, and the role of virtual care in improving maternal health.",[122,29,123,124],"Birth","Pregnancy","Maternal Health",[96,126,127,128,129,130],"virtual","doula","pregnancy","birth","maternal health","2025-12-18",{"date":133,"type":34},"2025-12-22",{"date":135,"type":19},"2026-09",{"date":137,"type":19},"2029-12",{"name":139,"class":41},"RAND",{"id":141,"slug":142,"hasResults":11,"nctId":143,"briefTitle":144,"officialTitle":145,"acronym":146,"eligibilityCriteria":147,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":148,"targetDuration":4,"studyType":20,"phases":150,"briefSummary":151,"conditions":152,"keywords":157,"overallStatus":60,"whyStopped":4,"lastUpdateSubmitDate":159,"lastUpdatePostDateStruct":160,"startDateStruct":162,"completionDateStruct":164,"leadSponsor":166,"locationsCount":168},"100590724","nurse-led-telehealth-for-gout-100590724","NCT06971146","Nurse-Led Telehealth for Gout","Health Literacy-Based, Nurse-Led Telehealth Support for Gout Self-Management: the Danish Randomized GOUTCONNECT Trial","GoutConnect","Inclusion Criteria:\n\n* ≥18 years old\n* Fulfills ACR\u002FEULAR 2015 Gout Classification Criteria\n* Estimated Glomerular Filtration Rate (e-GFR) \\>30 ml\u002Fmin\n* Prescribed Allopurinol or Adenuric, and achieved two consecutive serum urate levels of two consecutive serum urate levels of ≤0.30 mmol\u002Fl for patients with tophi and ≤0.36 mmol\u002FL for patients without tophi\n* Have sufficient Danish reading and writing skills to understand information and complete questionnaires.\n\nExclusion Criteria:\n\n• Cognitively impaired, unable to understand or provide informed consent.",{"count":149,"type":19},200,[22],"The aim of this clinical trial is to evaluate whether nurse-led telehealth support helps individuals with gout better manage their condition and adhere to urate-lowering medication after discharge from a rheumatology clinic.\n\nEligible patients will be recruited from five rheumatology departments in the Central Denmark Region after achieving two consecutive target serum urate levels-below 0.36 mmol\u002FL, or below 0.30 mmol\u002FL for patients with tophi.\n\nParticipants will be adults with gout who meet specific medical criteria, are taking medications such as allopurinol or Adenuric, and are able to read and write Danish.\n\nParticipants will be randomly assigned to one of two groups:\n\n* Intervention group: nurse-led telehealth support.\n* Control group: usual care with follow-up by their general practitioner.\n\nThe primary goal is to support patients in maintaining healthy uric acid levels after 52 weeks.\n\nParticipants in the nurse-led group have the option to choose from four support options:\n\nI1: App-Based Support - an app provides information and reminders. I2: Letter Reminders - messages are sent via digital or postal mail. I3: Text Reminders - SMS messages are sent every three months. I4: Phone Support - nurses call three times a year to check in.",[90,153,154,29,155,156],"Gout Arthritis","Gout Initiating Urate-loweringUrate-lowering Therapy","Digital Health","Adherence",[158],"self-managment","2025-09-17",{"date":161,"type":34},"2025-09-18",{"date":163,"type":19},"2025-10-01",{"date":165,"type":19},"2027-08-01",{"name":167,"class":41},"University of Aarhus",5,{"id":170,"slug":171,"hasResults":11,"nctId":172,"briefTitle":173,"officialTitle":174,"acronym":175,"eligibilityCriteria":176,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":177,"targetDuration":4,"studyType":20,"phases":179,"briefSummary":180,"conditions":181,"keywords":185,"overallStatus":60,"whyStopped":4,"lastUpdateSubmitDate":191,"lastUpdatePostDateStruct":192,"startDateStruct":194,"completionDateStruct":196,"leadSponsor":198,"locationsCount":42},"100592388","effectiveness-and-acceptability-of-remote-fine-tuning-of-hearing-aids-in-danish-adults-100592388","NCT06992778","Effectiveness and Acceptability of Remote Fine-Tuning of Hearing Aids in Danish Adults","Exploring the Effectiveness and Acceptability of Remote Fine-Tuning of Hearing Aids in Danish Adults: A Non-blinded, Non-inferiority Randomized Controlled Trial With an Embedded Qualitative Study","EARFit","Inclusion Criteria:\n\n* Adult patients with hearing loss who desire HA treatment (+18 of age).\n* Danish language skills both written and oral.\n* Acquisition of digital proficiency in terms of being familiar with operating a smartphone, including navigating menus, opening and closing apps, and interacting with the touchscreen with capabilities for audio and video calls.\n* Access to a smartphone that are compatible with manufacturers' system requirements.\n* Access to a stable network connection on the mobile device, with either Wi-Fi or mobile data.\n\nExclusion Criteria:\n\n* Patients with tinnitus requiring treatment or scoring more than 58 in the 'Tinnitus Handicap Inventory' (THI) grading system.\n* Patients with Ménière disease, due to its complications and symptoms as dizziness, balance problems and fluctuating hearing loss, that can affect the HA treatment.\n* Patients who will receive in-the-ear (ITE) hearing aids, due to potential limitations in connectivity for remote fine-tuning.\n* Patients which are recommended\u002Foffered unilateral HA treatment.",{"count":178,"type":19},120,[22],"The aim of this clinical trial is to evaluate the effectiveness and user satisfaction of remote fine-tuning of hearing aids compared to traditional face-to-face adjustments. The main questions aims to answer:\n\n\\- Are hearing aid outcomes (self-reported and objective) similar when using remote fine-tuning compared to face-to-face adjustments?\n\nResearchers will compare remote fine-tuning (using a smartphone app) to traditional face-to-face fine-tuning sessions in a clinical setting.\n\nParticipants will:\n\n* Be randomized to either the remote fine-tuning group (intervention group) or the face-to-face adjustment group (control group).\n* Attend five scheduled consultations over a 3-month period, including baseline measurements, hearing aid fittings, and follow-up visits.\n\nParticipants in the remote fine-tuning group will:\n\n\\- Set up and use a hearing aid manufacturer's smartphone app to complete fine-tuning sessions from home.\n\nParticipants in the face-to-face group will:\n\n\\- Visit the clinic for in-person fine-tuning appointments.\n\nData will be collected through questionnaires (e.g., SSQ-12, IOI-HA, and COSI) and objective measures such as the Speech Intelligibility Index (SII) and speech comprehension in noise (DS-FF). Additional qualitative data will be gathered from interviews with participants in the remote fine-tuning group.",[182,29,183,184],"Hearing Aid","Hearing Aid Fitting","Effectiveness",[186,187,188,189,190],"Remote fine-tuning","Teleaudiology","Randomized controlled trial (RCT)","Hearing aids","Denmark","2025-08-13",{"date":193,"type":34},"2025-08-14",{"date":195,"type":34},"2025-05-27",{"date":197,"type":19},"2026-03-30",{"name":199,"class":41},"Zealand University Hospital",{"id":201,"slug":202,"hasResults":11,"nctId":203,"briefTitle":204,"officialTitle":205,"acronym":4,"eligibilityCriteria":206,"healthyVolunteers":11,"sex":115,"minAge":16,"maxAge":207,"enrollmentInfo":208,"targetDuration":4,"studyType":20,"phases":210,"briefSummary":211,"conditions":212,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":216,"lastUpdatePostDateStruct":217,"startDateStruct":219,"completionDateStruct":221,"leadSponsor":223,"locationsCount":42},"100591333","health-education-for-women-with-suspeced-infertility-waiting-for-specialized-care-100591333","NCT06979063","Health Education for Women With Suspeced Infertility Waiting for Specialized Care","Impact of Regulation Strategies and Health Education for Managing Infertility in Primary Health Care in Rio Grande do Sul","Inclusion Criteria:\n\n* Individuals referred to specialized infertility care in Porto Alegre.\n* Age up to 33 years and 11 months.\n\nExclusion Criteria:\n\n* Lack of access to the internet or telephone.\n* Prior specialized infertility treatment in the private healthcare system.","34 Years",{"count":209,"type":19},206,[22],"Introduction: Infertility is defined as a couple's inability to achieve pregnancy after 12 months or more of regular unprotected intercourse. In Brazil, it affects around eight million people. While health services provide resources for contraception, little attention is given to supporting conception and preserving fertility.\n\nObjective: To evaluate the effectiveness of a remote educational and counseling intervention on infertility.\n\nMethod: Open-label randomized clinical trial. Couples referred for infertility will be identified in the electronic referral system. For inclusion, the woman of the couple must be 34 years old or less, no previous in-vitro fertilization attempts, and have access to telephone or internet. The control group will follow standard care, awaiting in-person consultation. The intervention group will also wait for in-person evaluation but receive additional education and counseling via video call.\n\nThe primary outcome is the proportion of correct referrals according to local protocols. A total of 206 participants will be included to detect a difference between success rates of 50% and 30%, with 80% power and a 5% significance level.",[213,214,215,29],"Infertility","Health Education","Telemedicine","2025-05-12",{"date":218,"type":34},"2025-05-18",{"date":220,"type":19},"2025-06",{"date":222,"type":19},"2026-12-31",{"name":224,"class":41},"Hospital de Clinicas de Porto Alegre",{"id":226,"slug":227,"hasResults":11,"nctId":228,"briefTitle":229,"officialTitle":230,"acronym":231,"eligibilityCriteria":232,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":233,"enrollmentInfo":234,"targetDuration":4,"studyType":20,"phases":236,"briefSummary":237,"conditions":238,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":242,"lastUpdatePostDateStruct":243,"startDateStruct":245,"completionDateStruct":247,"leadSponsor":248,"locationsCount":4},"100537090","towards-telemonitoring-in-immune-mediated-inflammatory-diseases-implementation-of-a-mixed-attention-model-imidoc-100537090","NCT06273306","Towards Telemonitoring in Immune-Mediated Inflammatory Diseases: Implementation of a Mixed Attention Model (IMIDOC)","Towards Telemonitoring in Immune-Mediated Inflammatory Diseases: Implementation of a Mixed Attention Model","IMIDOC","Inclusion Criteria:\n\n* Clinical diagnosis with Rheumatoid Arthritis or Spondylarthritis\n* Treatment with biologic or targeted disease modifying antirheumatic drugs.\n* Ability to use smartphone.\n\nExclusion Criteria:\n\n* only patients with conditions that hinder or prevent the use of a mobile application (blindness, mental retardation, dementia, digitalfilliteracy).","80 Years",{"count":235,"type":19},360,[22],"The main objective is to evaluate the implementation of a hybrid care model called the mixed attention model (MAM) in clinical practice and to evaluate whether its implementation improves clinical outcomes compared to conventional follow-up.\n\nThis is a multicenter prospective observational study involving 360 patients with rheumatoid arthritis (RA) and Spondylarthritis (SpA) from five Spanish Hospitals. Patients will be followed-up by the MAM protocol, which is a care model that incorporates the use of digital tool consisting of a mobile application (App) that patients can use at home and that professionals can review asynchronously to detect incidents and to follow their patients; clinical evolution between face-to-face visits. Another group of patients, whose follow-up will be conducted in accordance with a traditional face-to-face care model, will be assessed as the control group. Sociodemographic characteristics, treatments, laboratory parameters, assessment of tender and swollen joints, visual analogue scale for pain and electronic patient reported outcome reports (ePROs) will be collected for all subjects. In the MAM group, these items will be self-assessed both by the mobile App and during face-to-face visits with rheumatologist, who will do the same for patients included in the traditional care model. Patients will be able to report any incidence related to their disease or treatment through the mobile App.",[215,29,89,239,240,241],"Rheumatic Diseases","Arthritis, Rheumatoid","Spondylarthritis","2024-02-15",{"date":244,"type":34},"2024-02-22",{"date":246,"type":19},"2024-03-15",{"date":222,"type":19},{"name":249,"class":41},"Instituto de Investigación Hospital Universitario La Paz"]